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Diverse methods are employed to manipulate the initiation, propagation, and termination rates during chain polymerization. A related issue is temperature control, also called heat management, during these reactions, which are often highly exothermic. For example, for the polymerization of ethylene, 93.6 kJ of energy are released per mole of ...
The easiest way to visualize the mechanism of a step-growth polymerization is a group of people reaching out to hold their hands to form a human chain—each person has two hands (= reactive sites). There also is the possibility to have more than two reactive sites on a monomer: In this case branched polymers production take place.
RAFT agent Z groups in decreasing order of reactivity. Recommended monomers: 1-4: MMA, HPMAM; 5: MMA, HPMAM (partial control); 7-11: VAc, NVP; 1-6: St, MA, AM, AN; 7-10: St, MA, AM, AN (partial control) Guidelines have been provided for selection of R and Z groups based on the monomer to be polymerised and these are summarised in Figures 6 and 7.
Note that different copolymer sequencing is sufficient to define a structural difference, thus an A-B diblock copolymer with A-B alternating copolymer side chains is properly called a graft copolymer. For example, polystyrene chains may be grafted onto polybutadiene, a synthetic rubber which retains one reactive C=C double bond per repeat unit.
In one copolymer, the monomers can be almost perfectly alternating. [1] but (random) copolymerisation with less than 50% maleic anhydride content is also possible. [2] The polymer is formed by a radical polymerization, using an organic peroxide as the initiator. The main characteristics of SMA copolymer are its transparent appearance, high heat ...
For the copolymerization of a given pair of monomers, the two experimental reactivity ratios r 1 and r 2 permit the evaluation of (Q 1 /Q 2) and (e 1 – e 2). Values for each monomer can then be assigned relative to a reference monomer, usually chosen as styrene with the arbitrary values Q = 1.0 and e = –0.8. [28]
Maleic acid in fact does not homopolymerize in free radical polymerization, but will form an almost exclusively alternating copolymer with styrene. [8] >> >> In the initial stage of the copolymerization, monomer 1 is incorporated faster and the copolymer is rich in monomer 1. When this monomer gets depleted, more monomer 2 segments are added.
It is one of the most developed methods in chain-growth polymerization. Currently, most polymers in our daily life are synthesized by free radical polymerization, including polyethylene, polystyrene, polyvinyl chloride, polymethyl methacrylate, polyacrylonitrile, polyvinyl acetate, styrene butadiene rubber, nitrile rubber, neoprene, etc.